State

Washington product recalls

73,576 recalls have nationwide distribution and so reach Washington. 8,466 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,466
Critical: 868
Severe: 2,396
Most recent: 2026-10-21

Of the 8,466 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,466 recalls whose distribution notice names Washington specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25876–25900 of 82042

HighCPSC·21782·2021-09-16
Harbor Freight Tools Bauer Propane Portable Heaters Fire Hazard
Harbor Freight Tools is recalling about 19,000 Bauer Forced Air Propane Portable Heaters because the fitting at the back can fail to be sufficiently tight, causing propane gas leaks and posing a fire hazard. The firm has received 13 reports of gas leaking, including one fire report, with no injuries reported.
Product
Bauer Forced Air Propane Portable Heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V722000·2021-09-16
Altec Recalls 2016-2021 Aerial Devices Due to Bearing Bolt Defect
Altec is recalling 2016-2021 LS87 aerial devices because bearing bolt washers may interfere with welds, causing bolts to break and increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21783·2021-09-16
Textron E-Z-GO and Tracker Off-Road Vehicles Recalled for Parking Brake Failure
Textron Specialized Vehicles recalled approximately 6,600 E-Z-GO PTVs and Tracker Off-Road Vehicles because the parking brake catch bracket can wear out and fail, creating a crash hazard. Consumers should stop using the vehicles immediately.
Product
E-Z-GO PTVs and Tracker Off-Road Vehicles
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V721000·2021-09-16
Vermeer and McLaughlin Vacuum Excavators Recalled for Lighting Defects
Vermeer is recalling 2005-2021 McLaughlin and 2021 Vermeer vacuum excavators because rear clearance lamps and reflectors are insufficient, increasing crash risk.
Product
VERMEER — VERMEER, MCLAUGHLIN VACUUM EXCAVATOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2402-2021·2021-09-15
Pipeline Flex Embolization Device Recalled for Potential Push Wire Fracture Risk
Micro Therapeutics recalls Pipeline Flex Embolization Devices for potential push wire fractures in the delivery system during use. Device fractures in the Hypotube may result in malfunction during vascular procedures.
Product
Pipeline Flex Embolization Device
Category
Medical Device
Distribution
49 states
SevereFDA (Devices)·Z-2377-2021·2021-09-15
NORMOFLO Irrigation Warming Sets Recalled for Aluminum Leaching Risk
Smiths Medical is recalling NORMOFLO Irrigation Warming sets (Models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700) due to potential aluminum leaching when used at lower flow rates with certain solutions and blood products. No illnesses have been reported.
Product
NORMOFLO Irrigation Warming administration set (disposable), Models IR-40, IR-500, IR-600, IRI-600, IRI-600B, IR-700
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V716000·2021-09-15
Volvo Recalls S90, XC60, and XC90 Models for Brake System Defect
Volvo is recalling 2020-2021 S90, XC60, and XC90 vehicles because a brake component may separate, potentially reducing braking assistance and increasing crash risk.
Product
VOLVO — VOLVO XC60, XC90, S90
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2403-2021·2021-09-15
EV3 Pipeline Flex Embolization Device Recalled for Push Wire Fracture Risk
Micro Therapeutics Inc. is recalling 16,169 EV3 Pipeline Flex Embolization Devices due to potential push wire fractures in the delivery system during use.
Product
EV3 Pipeline Flex Embolization Device with Flex Shield Technology
Category
Medical Device
Distribution
49 states
SevereFDA (Devices)·Z-2376-2021·2021-09-15
NORMOFLO Irrigation Fluid Warmer Recalled for Risk of Aluminum Leaching
Smiths Medical recalls NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129 (913 units) due to potential harmful aluminum leaching when used at lower flow rates with certain solutions and blood products.
Product
NORMOFLO Irrigation Fluid Warmer Models H-1100 and H-1129
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2419-2021·2021-09-15
MRI Tabletop May Not Move Properly in Manual Mode
The patient tabletop on affected Philips Ingenia Elition MRI systems may not move completely in or out during manual operation, potentially delaying patient evacuation from the device.
Product
Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2418-2021·2021-09-15
MRI Magnetic Resonance System Tabletop May Fail to Move in Manual Mode
Philips Ingenia Elition S-a MRI systems may have tabletop movement failure in manual mode, potentially delaying patient evacuation from the scanner bore and treatment. This affects 64 units distributed worldwide.
Product
Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2413-2021·2021-09-15
MRI device tabletop may fail to move completely in manual mode
Philips Ingenia MRI tabletops may fail to move completely in manual mode, potentially delaying patient evacuation. The recall affects 144 units worldwide.
Product
Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2424-2021·2021-09-15
Atellica IM Diagnostic Test Kit Recalled for Calibration Interval Deficiency
Siemens Healthcare recalls the Atellica IM BR 27.29 diagnostic test kit because it does not maintain the claimed 10-day calibration interval; the required interval has been shortened to 3 days to ensure accurate results.
Product
Atellica IM BR 27.29 (BR) Assay 50 Test Kit- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer. SMN: 10995478
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2427-2021·2021-09-15
Philips HEARTSTART Infant/Child Defibrillator Pads Recalled for Incorrect Labeling
Philips infant/child defibrillator pads are recalled due to incorrect labeling that could delay therapy or result in lower energy delivery than indicated.
Product
Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123, NON-STERILE, Rx only, UDI: (01) 00884838023758 for use with defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V715000·2021-09-15
2022 Freightliner Cascadia Trucks Recalled for Exhaust Pipe Fire Risk
Certain 2022 Freightliner Cascadia trucks are being recalled because the exhaust pipe outlet may be improperly installed, with the tip facing the battery box. Exhaust heat could melt the battery box, creating a fire risk.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2416-2021·2021-09-15
Ingenia Ambition S-a MRI System tabletop may not move in manual mode
The Philips Ingenia Ambition S-a MRI system may not fully move its patient tabletop in or out of the bore during manual mode operation, potentially delaying patient evacuation and treatment.
Product
Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2421-2021·2021-09-15
MRI Tabletop Movement Failure May Delay Patient Evacuation and Treatment
Philips MRI systems may fail to move the examination tabletop in manual mode, potentially delaying patient evacuation and medical treatment.
Product
SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2422-2021·2021-09-15
Philips Ingenia Ambition X MRI System Tabletop May Fail to Retract
Philips Ingenia Ambition X MRI systems may have tabletops that fail to move completely in manual mode, potentially delaying patient evacuation from the scanner and treatment. The issue affects 147 units distributed worldwide.
Product
Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2412-2021·2021-09-15
Philips Ingenia 1.5T MRI tabletop malfunction may delay patient evacuation
Philips is recalling 42 Ingenia 1.5T MRI systems because the tabletop may not fully move in or out in manual mode, potentially delaying patient evacuation and treatment.
Product
Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2420-2021·2021-09-15
Medical Device Alert: Philips Ingenia MRI Tabletop Movement Failure
Philips Ingenia 3.0T MRI systems may fail to move the patient tabletop completely in or out, potentially delaying patient evacuation and treatment. 266 units are affected worldwide.
Product
Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0956-2021·2021-09-15
Fermentation Derived Pepsin recalled for undeclared egg allergen
Ingredion is recalling Fermentation Derived Pepsin due to undeclared egg allergen. The affected product was distributed across multiple U.S. states.
Product
Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample bags packaged in 25 kg HDPE Drums
Category
Food
Distribution
10 states
HighNHTSA·21V714000·2021-09-15
2022 Thomas Built Buses Saf-T-Liner HDX Recalled for Fan Belt Defect
Daimler Trucks North America is recalling 50 model-year 2022 Thomas Built Buses Saf-T-Liner HDX school buses because fan drive pulley assembly bolts may be incorrect or improperly installed, potentially causing a disabled bus.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0959-2021·2021-09-15
Trader Joe's Super Spinach Salad recalled for undeclared almonds
Trader Joe's Super Spinach Salad packages were prepared using almonds instead of the declared pumpkin seeds, creating an undeclared allergen hazard for consumers with nut allergies.
Product
Trader Joe's Super Spinach Salad with Quinoa, carrots, cranberries, chickpeas, edamame, pumpkin seeds and a carrot ginger miso dressing. Net Wt. 10 oz. (284 g) Dressing and seeds/nuts are packed in separate clear pouches and visible to consumer. Contains: Soy UPC: 096155 SKU…
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2423-2021·2021-09-15
Arc Endocuff Vision endoscopic device recalled for packaging seal defects
Olympus recalls Arc Endocuff Vision endoscopic devices for packaging seal defects that may breach sterile barriers, risking patient infection. Approximately 711,157 units nationwide are affected.
Product
Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8, Part Number: E0420501; ARV120 ENDOCUFF-V L GREEN PK8, Part Number: E0420500; ARV130 ENDOCUFF-V S PURPLE PK8, Part Number: E0420502; ARV140 ENDOCUFF-V XL ORANGE PK8 ARV110, Part Number: E0420503 Intended to be…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2425-2021·2021-09-15
Medical Device Test Kit Requires More Frequent Calibration Than Labeled
Siemens Atellica IM BR 27.29 test kit requires calibration every 3 days instead of the labeled 10-day interval. The product's calibration performance does not meet its Instructions for Use specifications.
Product
Atellica IM BR 27.29 (BR) Assay 250 Test Kit- in vitro diagnostic use in the quantitative serial determination of cancer antigen CA 27.29 in human serum and plasma (EDTA) using the Atellica IM Analyzer. SMN: 10995477
Category
Medical Device
Distribution
Distributed nationwide